Canonical Allele Identifier: CA384104129
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174611T>A , CM000674.2:g.21174611T>A GRCh38
NC_000012.11:g.21327545T>A , CM000674.1:g.21327545T>A GRCh37
NC_000012.10:g.21218812T>A NCBI36
NG_011745.1:g.48418T>A , LRG_1022:g.48418T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.261T>A MANE Select ENSP00000256958.2:p.Phe87Leu
ENST00000256958.2:c.261T>A ENSP00000256958.2:p.Phe87Leu
ENST00000543498.5:c.426-2165T>A
NM_006446.4:c.261T>A , LRG_1022t1:c.261T>A NP_006437.3:p.Phe87Leu
NM_006446.5:c.261T>A MANE Select NP_006437.3:p.Phe87Leu